Article info
Online mutation report
Novel mutations in COX15 in a long surviving Leigh syndrome patient with cytochrome c oxidase deficiency
- Correspondence to: Massimo Zeviani Department of Molecular Neurogenetics, Istituto Nazionale Neurologico “C. Besta”, via Libero Temolo, 4 20126 Milano, Italy; zevianiistituto-besta.it
Citation
Novel mutations in COX15 in a long surviving Leigh syndrome patient with cytochrome c oxidase deficiency
Publication history
- Accepted December 17, 2004
- Revised December 10, 2004
- First published April 29, 2005.
Online issue publication
April 29, 2005
Request permissions
If you wish to reuse any or all of this article please use the link below which will take you to the Copyright Clearance Center’s RightsLink service. You will be able to get a quick price and instant permission to reuse the content in many different ways.
Copyright information
Copyright 2005 Journal of Medical Genetics